Visible-light-mediated synthesis of oxime esters <i>via</i> multicomponent reactions of aldehydes, aryl amines, and <i>N</i>-hydroxyphthalimide esters

Nguyen, Anh Thu; Kim, Hee-Kwon

doi:10.1039/d3ra06737h

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2024

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Cited by 7 publications

(1 citation statement)

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“…Aniline is an important intermediate in syntheses of organic chemical raw materials that are widely used in organic dyes, pesticides, pharmaceuticals and textiles. 1–7 Nitrobenzene hydrogenation is a common method for industrial aniline production. Traditional metal catalysts generally have high catalytic activity, but often have poor stability and cannot be reused.…”

Section: Introductionmentioning

confidence: 99%

Nitrogen-doped carbon material NCM-T heterogeneously catalyzed liquid-phase hydrogenation of nitrobenzene to aniline

Gao,

Liu

et al. 2024

RSC Adv.

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Section: Introductionmentioning

confidence: 99%

Nitrogen-doped carbon material NCM-T heterogeneously catalyzed liquid-phase hydrogenation of nitrobenzene to aniline

Gao,

Liu

et al. 2024

RSC Adv.

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Recent progress in visible light‐driven halogenation: Chlorination, bromination, and iodination

Nguyen,

Kang,

Luu

et al. 2024

Bulletin Korean Chem Soc

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Halogenation is one of the most important transformations in organic synthesis. Halogenated compounds are employed in many reactions to prepare useful molecules. Many methods have been developed to introduce halogens into different compounds. Visible light‐mediated reactions are the efficient, low‐toxic, and mild‐condition methods applied for various organic chemistry transformations. Remarkably, there has been an increasing development in the application of visible light‐induced halogenation in recent years. Herein, we present a comprehensive summary of halogenation reactions including chlorination, bromination, and iodination under visible light irradiation since 2020.

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Solvent‐Free Synthesis of Carvone Oxime Ester and Carvone Oxime Sulfonic Esters

Yang,

Yan,

Zeng

et al. 2024

ChemistrySelect

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A ZnO‐mediated benzoylation between carvone oxime and acyl is reported, enabling access to diverse carvone oxime ester and carvone oxime sulfonic esters under solvent‐free conditions. The operationally simple procedure provides a novel method for the synthesis of oxime‐ester bonds with excellent chemo selectivity. This strategy provides a mild, direct, and green approach for synthesizing carvone oxime ester in moderate to excellent yields with good substrate tolerance. In addition, carvone oxime was synthesized under solvent‐free conditions.

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Visible-light-mediated synthesis of oxime esters via multicomponent reactions of aldehydes, aryl amines, and N-hydroxyphthalimide esters

Abstract: Practical and efficient visible-light-induced synthesis of oxime esters has been achieved via multicomponent reactions in the presence of catalytic eosin Y.

Cited by 7 publications

References 70 publications

Nitrogen-doped carbon material NCM-T heterogeneously catalyzed liquid-phase hydrogenation of nitrobenzene to aniline

Nitrogen-doped carbon material NCM-T heterogeneously catalyzed liquid-phase hydrogenation of nitrobenzene to aniline

Recent progress in visible light‐driven halogenation: Chlorination, bromination, and iodination

Solvent‐Free Synthesis of Carvone Oxime Ester and Carvone Oxime Sulfonic Esters

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